This allele was generated at The Jackson Laboratory by electroporating Cas9 protein and 2 guide sequences TGTCCTGTCTACAAATCTTG and CACTCCATAAACATGTTCCG, which resulted in a 1789 bp deletion beginning at Chromosome 1 position 163,995,732 bp and ending after 163,997,520 bp (GRCm38/mm10). This mutation deletes ENSMUSE00000688041 (exon 2) and 459 bp of flanking intronic sequence including the splice acceptor and donor and is predicted to cause a null allele. There is a 14 bp insertion at the deletion site (GTAGTATGTAGAGTA). (J:188991)
Legend:
cx: complex: > 1 genome feature ot: other: hemizygous, indeterminate,... (F): Female
(M): Male
N: normal phenotype
(#): related diseases count